Similarities between Pyruvate dehydrogenase and Pyruvate dehydrogenase (lipoamide) beta
Pyruvate dehydrogenase and Pyruvate dehydrogenase (lipoamide) beta have 8 things in common (in Unionpedia): Acetyl-CoA, Adenosine triphosphate, Citric acid cycle, Dihydrolipoyl transacetylase, Glycolysis, Pyruvate dehydrogenase deficiency, Pyruvic acid, Thiamine pyrophosphate.
Acetyl-CoA
Acetyl-CoA (acetyl coenzyme A) is a molecule that participates in many biochemical reactions in protein, carbohydrate and lipid metabolism.
Acetyl-CoA and Pyruvate dehydrogenase · Acetyl-CoA and Pyruvate dehydrogenase (lipoamide) beta ·
Adenosine triphosphate
Adenosine triphosphate (ATP) is a complex organic chemical that participates in many processes.
Adenosine triphosphate and Pyruvate dehydrogenase · Adenosine triphosphate and Pyruvate dehydrogenase (lipoamide) beta ·
Citric acid cycle
The citric acid cycle (CAC) – also known as the tricarboxylic acid (TCA) cycle or the Krebs cycle – is a series of chemical reactions used by all aerobic organisms to release stored energy through the oxidation of acetyl-CoA derived from carbohydrates, fats, and proteins into carbon dioxide and chemical energy in the form of adenosine triphosphate (ATP).
Citric acid cycle and Pyruvate dehydrogenase · Citric acid cycle and Pyruvate dehydrogenase (lipoamide) beta ·
Dihydrolipoyl transacetylase
Dihydrolipoyl transacetylase (or dihydrolipoamide acetyltransferase) is an enzyme component of the multienzyme pyruvate dehydrogenase complex.
Dihydrolipoyl transacetylase and Pyruvate dehydrogenase · Dihydrolipoyl transacetylase and Pyruvate dehydrogenase (lipoamide) beta ·
Glycolysis
Glycolysis (from glycose, an older term for glucose + -lysis degradation) is the metabolic pathway that converts glucose C6H12O6, into pyruvate, CH3COCOO− + H+.
Glycolysis and Pyruvate dehydrogenase · Glycolysis and Pyruvate dehydrogenase (lipoamide) beta ·
Pyruvate dehydrogenase deficiency
Pyruvate dehydrogenase deficiency (also known as pyruvate dehydrogenase complex deficiency or PDCD) is one of the most common neurodegenerative disorders associated with abnormal mitochondrial metabolism.
Pyruvate dehydrogenase and Pyruvate dehydrogenase deficiency · Pyruvate dehydrogenase (lipoamide) beta and Pyruvate dehydrogenase deficiency ·
Pyruvic acid
Pyruvic acid (CH3COCOOH) is the simplest of the alpha-keto acids, with a carboxylic acid and a ketone functional group.
Pyruvate dehydrogenase and Pyruvic acid · Pyruvate dehydrogenase (lipoamide) beta and Pyruvic acid ·
Thiamine pyrophosphate
Thiamine pyrophosphate (TPP or ThPP), or thiamine diphosphate (ThDP), or cocarboxylase is a thiamine (vitamin B1) derivative which is produced by the enzyme thiamine diphosphokinase.
Pyruvate dehydrogenase and Thiamine pyrophosphate · Pyruvate dehydrogenase (lipoamide) beta and Thiamine pyrophosphate ·
The list above answers the following questions
- What Pyruvate dehydrogenase and Pyruvate dehydrogenase (lipoamide) beta have in common
- What are the similarities between Pyruvate dehydrogenase and Pyruvate dehydrogenase (lipoamide) beta
Pyruvate dehydrogenase and Pyruvate dehydrogenase (lipoamide) beta Comparison
Pyruvate dehydrogenase has 40 relations, while Pyruvate dehydrogenase (lipoamide) beta has 23. As they have in common 8, the Jaccard index is 12.70% = 8 / (40 + 23).
References
This article shows the relationship between Pyruvate dehydrogenase and Pyruvate dehydrogenase (lipoamide) beta. To access each article from which the information was extracted, please visit: